Conmed Corporation: Insufflator, Laparoscopic
Recall Summary ConMed Corporation is recalling specific laparoscopic surgical equipment (AirSeal 8mm Access Port and related components) distributed nationwide because the carbon dioxide insufflator may not properly alert when pressure becomes too high during surgery. This recall affects medical facilities that received these products, which are used in minimally invasive abdominal procedures.
- Recalling firm
- ConMed Corporation
- Product
- ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS8-100LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.
- Reason
- Potential for overpressure alerts.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-05-14
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- Nationwide distribution
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/9307efb3-5b04-4a46-8c19-eee1a3b04ebb